Calquence: Has anyone been on Calquence. How is... - CLL Support

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Calquence

PThomas profile image
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Has anyone been on Calquence. How is it compares to Imbruvica?

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PThomas
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lankisterguy profile image
lankisterguyVolunteer

Please look for the box on this page labeled: "Related Posts

*Calquence - new clinical trial?

*Calquence approved in Canada for CLL?

*Calquence side effects

*Side effects of Calquence

*Anyone taking calquence (acalabrutinib)?

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Len

AussieNeil profile image
AussieNeilPartnerAdministrator

Did you see yesterday's post?

healthunlocked.com/cllsuppo...

Why the sudden interest in Acalabrutinb/Calquence after 3 years on Ibrutinib? How are your nodes and blood counts now?

Neil

Virgo10 profile image
Virgo10

I switched from ibrutinib to calquence because the form severely aggravated my osteoporosis arthritis. No side effects with calquence.

bulldozer4264 profile image
bulldozer4264

Wifey was on Ibrutinib for 5 years. Pain (Arthralgia) got slowly worse over those years. Switched to Calquence 8 months ago. Pain much better. Other side effects still the same.

Italianpainter profile image
Italianpainter

I was on Imbruvica for almost 10 months. Shortly after starting it I developed red painful swellings under the skin that would go away 2 to 4 weeks later. It wasnt until about 9 months into it that a pharmacist found out what they were. Panniculitis and it occurs in less than 1% of people on Imbruvica. Then near the end of my treatment with imbruvica I developed blisters on 8 of my 10 fingers. Remarkably painful. That same pharmacist called my oncologist about both situations and got him to stop the drug. I also had lots of musculoskeletal pain for the entire time on it.

I started acalabrutinib a week ago and have only headaches, which are pretty bad, but that's all so far. I'm not sure which is worse, the treatment or the disease.

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